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      Dysbiosis and Its Discontents

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          ABSTRACT

          Dysbiosis is a key term in human microbiome research, especially when microbiome patterns are associated with disease states. Although some questions have been raised about how this term is applied, its use continues undiminished in the literature. We investigate the ways in which microbiome researchers discuss dysbiosis and then assess the impact of different concepts of dysbiosis on microbiome research. After an overview of the term’s historical roots, we conduct quantitative and qualitative analyses of a large selection of contemporary dysbiosis statements. We categorize both short definitions and longer conceptual statements about dysbiosis. Further analysis allows us to identify the problematic implications of how dysbiosis is used, particularly with regard to causal hypotheses and normal-abnormal distinctions. We suggest that researchers should reflect carefully on the ways in which they discuss dysbiosis, in order for the field to continue to develop greater predictive scope and explanatory depth.

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          Most cited references43

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          Defining a healthy human gut microbiome: current concepts, future directions, and clinical applications.

          Indigenous microbiota are an essential component in the modern concept of human health, but the composition and functional characteristics of a healthy microbiome remain to be precisely defined. Patterns of microbial colonization associated with disease states have been documented, but the health-associated microbial patterns and their functional characteristics are less clear. A healthy microbiome, considered in the context of body habitat or body site, could be described in terms of ecologic stability (i.e., ability to resist community structure change under stress or to rapidly return to baseline following a stress-related change), by an idealized (presumably health-associated) composition or by a desirable functional profile (including metabolic and trophic provisions to the host). Elucidation of the properties of healthy microbiota would provide a target for dietary interventions and/or microbial modifications aimed at sustaining health in generally healthy populations and improving the health of individuals exhibiting disrupted microbiota and associated diseases. Copyright © 2012 Elsevier Inc. All rights reserved.
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            Antibiotics, pediatric dysbiosis, and disease.

            Antibiotics are by far the most common medications prescribed for children. Recent epidemiological data suggests an association between early antibiotic use and disease phenotypes in adulthood. Antibiotic use during infancy induces imbalances in gut microbiota, called dysbiosis. The gut microbiome's responses to antibiotics and its potential link to disease development are especially complex to study in the changing infant gut. Here, we synthesize current knowledge linking antibiotics, dysbiosis, and disease and propose a framework for studying antibiotic-related dysbiosis in children. We recommend future studies into the microbiome-mediated effects of antibiotics focused on four types of dysbiosis: loss of keystone taxa, loss of diversity, shifts in metabolic capacity, and blooms of pathogens. Establishment of a large and diverse baseline cohort to define healthy infant microbiome development is essential to advancing diagnosis, interpretation, and eventual treatment of pediatric dysbiosis. This approach will also help provide evidence-based recommendations for antibiotic usage in infancy.
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              Advances in inflammatory bowel disease pathogenesis: linking host genetics and the microbiome.

              Studies of the genetics underlying inflammatory bowel diseases have increased our understanding of the pathways involved in both ulcerative colitis and Crohn's disease and focused attention on the role of the microbiome in these diseases. Full understanding of pathogenesis will require a comprehensive grasp of the delicate homeostasis between gut bacteria and the human host. In this review, we present current evidence of microbiome-gene interactions in the context of other known risk factors and mechanisms, and describe the next steps necessary to pair genetic variant and microbiome sequencing data from patient cohorts. We discuss the concept of dysbiosis, proposing that the functional composition of the gut microbiome may provide a more consistent definition of dysbiosis and may more readily provide evidence of genome-microbiome interactions in future exploratory studies.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                mBio
                MBio
                mbio
                mbio
                mBio
                mBio
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                2150-7511
                10 October 2017
                Sep-Oct 2017
                : 8
                : 5
                : e01492-17
                Affiliations
                [a ]Centre de Bioinformatique de Bordeaux, Centre de Génomique Fonctionnelle de Bordeaux, University of Bordeaux, Bordeaux, France
                [b ]Immunoconcept, CNRS UMR 5164, University of Bordeaux, Bordeaux, France
                University of British Columbia
                Author notes
                Address correspondence to Katarzyna B. Hooks, katarzyna.hooks@ 123456u-bordeaux.fr , or Maureen A. O’Malley, maureen.omalley@ 123456u-bordeaux.fr .
                Author information
                http://orcid.org/0000-0003-0687-4393
                Article
                mBio01492-17
                10.1128/mBio.01492-17
                5635691
                29018121
                4d6d62eb-28c7-46e9-a67d-2fd54532d9d9
                Copyright © 2017 Hooks and O’Malley.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

                History
                Page count
                supplementary-material: 4, Figures: 3, Tables: 0, Equations: 0, References: 74, Pages: 11, Words: 7381
                Funding
                Funded by: Agence Nationale de la Recherche (ANR) https://doi.org/10.13039/501100001665
                Award ID: ANR-10-IDEX-03-02
                Award Recipient : Maureen O'Malley
                Categories
                Perspective
                Custom metadata
                September/October 2017

                Life sciences
                dysbiosis,homeostasis,microbial diversity,microbiome,microbiota
                Life sciences
                dysbiosis, homeostasis, microbial diversity, microbiome, microbiota

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